A comparison of monodomain and bidomain reaction-diffusion models for action potential propagation in the human heart
- PMID: 17153199
- DOI: 10.1109/TBME.2006.880875
A comparison of monodomain and bidomain reaction-diffusion models for action potential propagation in the human heart
Abstract
A bidomain reaction-diffusion model of the human heart was developed, and potentials resulting from normal depolarization and repolarization were compared with results from a compatible monodomain model. Comparisons were made for an empty isolated heart and for a heart with fluid-filled ventricles. Both sinus rhythm and ectopic activation were simulated. The bidomain model took 2 days on 32 processors to simulate a complete cardiac cycle. Differences between monodomain and bidomain results were extremely small, even for the extracellular potentials, which in case of the monodomain model were computed with a high-resolution forward model. Propagation of activation was 2% faster in the bidomain model than in the monodomain model. Electrograms computed with monodomain and bidomain models were visually indistinguishable. We conclude that, in the absence of applied currents, propagating action potentials on the scale of a human heart can be studied with a monodomain model.
Similar articles
-
A comparison of monodomain and bidomain propagation models for the human heart.Conf Proc IEEE Eng Med Biol Soc. 2006;2006:3895-8. doi: 10.1109/IEMBS.2006.259484. Conf Proc IEEE Eng Med Biol Soc. 2006. PMID: 17945813
-
Analytical model of extracellular potentials in a tissue slab with a finite bath.IEEE Trans Biomed Eng. 2005 Feb;52(2):334-8. doi: 10.1109/TBME.2004.840467. IEEE Trans Biomed Eng. 2005. PMID: 15709672
-
An efficient numerical technique for the solution of the monodomain and bidomain equations.IEEE Trans Biomed Eng. 2006 Nov;53(11):2139-47. doi: 10.1109/TBME.2006.879425. IEEE Trans Biomed Eng. 2006. PMID: 17073318
-
Crosstalk between theoretical and experimental studies for the understanding of cardiac electrical impulse propagation.J Electrocardiol. 2007 Nov-Dec;40(6 Suppl):S136-41. doi: 10.1016/j.jelectrocard.2007.05.026. J Electrocardiol. 2007. PMID: 17993310 Review. No abstract available.
-
Basic mechanisms of cardiac impulse propagation and associated arrhythmias.Physiol Rev. 2004 Apr;84(2):431-88. doi: 10.1152/physrev.00025.2003. Physiol Rev. 2004. PMID: 15044680 Review.
Cited by
-
In silico investigation of the short QT syndrome, using human ventricle models incorporating electromechanical coupling.Front Physiol. 2013 Jul 5;4:166. doi: 10.3389/fphys.2013.00166. eCollection 2013. Front Physiol. 2013. PMID: 23847545 Free PMC article.
-
A Reproducible Protocol to Assess Arrhythmia Vulnerability in silico: Pacing at the End of the Effective Refractory Period.Front Physiol. 2021 Apr 1;12:656411. doi: 10.3389/fphys.2021.656411. eCollection 2021. Front Physiol. 2021. PMID: 33868025 Free PMC article.
-
Coupled agent-based and hyperelastic modelling of the left ventricle post-myocardial infarction.Int J Numer Method Biomed Eng. 2019 Jan;35(1):e3155. doi: 10.1002/cnm.3155. Epub 2018 Oct 22. Int J Numer Method Biomed Eng. 2019. PMID: 30253447 Free PMC article.
-
From Millimeters to Micrometers; Re-introducing Myocytes in Models of Cardiac Electrophysiology.Front Physiol. 2021 Oct 27;12:763584. doi: 10.3389/fphys.2021.763584. eCollection 2021. Front Physiol. 2021. PMID: 34777021 Free PMC article.
-
Modeling the role of the coronary vasculature during external field stimulation.IEEE Trans Biomed Eng. 2010 Oct;57(10):2335-45. doi: 10.1109/TBME.2010.2051227. Epub 2010 Jun 10. IEEE Trans Biomed Eng. 2010. PMID: 20542762 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources